A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415566



Internal ID194823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150879700..150879973hg38UCSC Ensembl
chrX:150048173..150048446hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737963
Samples
Known GenesCD99L2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415566
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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